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Microwave Based Synthesis; Structural, Optical and Magnetic Measurements of Co2+ Doped MnFe2O4

机译:微波合成Co2 +掺杂MnFe2O4的结构,光学和磁性测量

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Co2+ doped manganese ferrite (Mn1-xCoxFe2O4, x = 0.0, 0.1, 0.2, 0.3, 0.4, 0.5) samples were synthesized by a microwave combustion method. Nitrates of the constituent elements and urea were respectively used as the oxidizer and fuel to drive the reaction. On an average a yield of 80% were obtained for all the compositions. Light-absorbing properties from UV-Vis diffuse reflection spectrum were studied and the results infer that the band gap energy (E-g) of the pure MnFe2O4 is 1.76 eV and with increase in Co2+ ion concentration, it increases to 2.25 eV. The phase purity and crystal lattice symmetry were estimated from X-ray diffraction (XRD) and was identified as the spinel cubic crystal structure. The lattice parameter is found to decrease with an increase in Co content. The crystallite size was in the range of 19-25 nm. The purity and the composition of the elements were further confirmed by energy dispersive X-ray (EDX) results. Microstructural features obtained by scanning electron microscope (SEM) demonstrate that the nanocrystals were formed with a decrease in average grain size with Co2+ content. Room temperature magnetic measurement for stoichiometric samples is discussed with the help of vibrating sample magnetometer (VSM). The saturation magnetization (M-s), remanant magnetization (M-r) and coercivity (H-c) are measured from the respective hysteresis plots.
机译:通过微波燃烧法合成了Co2 +掺杂锰铁氧体(Mn1-xCoxFe2O4,x = 0.0,0.1,0.2,0.3,0.4,0.5)样品。构成元素的硝酸盐和尿素分别用作氧化剂和燃料来驱动反应。所有组合物平均获得80%的产率。研究了UV-Vis漫反射光谱的光吸收特性,结果表明,纯MnFe2O4的带隙能量(E-g)为1.76 eV,并且随着Co2 +离子浓度的增加,其增加至2.25 eV。通过X射线衍射(XRD)估计相纯度和晶格对称性,并将其鉴定为尖晶石立方晶体结构。发现晶格参数随着Co含量的增加而降低。微晶尺寸在19-25nm的范围内。元素的纯度和组成由能量色散X射线(EDX)结果进一步证实。通过扫描电子显微镜(SEM)获得的微结构特征表明,形成的纳米晶体具有随Co 2+含量而降低的平均晶粒尺寸。借助振动样品磁力计(VSM)讨论了化学计量样品的室温磁测量。根据各自的磁滞曲线测量饱和磁化强度(M-s),剩余磁化强度(M-r)和矫顽力(H-c)。

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